(9S)-Cinchonan-9-ol sulfate (2:1)
(9S)-Cinchonan-9-ol sulfate (2:1) structure
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Common Name | (9S)-Cinchonan-9-ol sulfate (2:1) | ||
|---|---|---|---|---|
| CAS Number | 5949-16-6 | Molecular Weight | 686.860 | |
| Density | 1.61g/cm3 | Boiling Point | 169 °C(lit.) | |
| Molecular Formula | C38H46N4O6S | Melting Point | 38-40 °C(lit.) | |
| MSDS | USA | Flash Point | 148 °F | |
| Purity | Quantity | Budget | Inquiry |
|---|
| Name | Cinchonine Sulfate Dihydrate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.61g/cm3 |
|---|---|
| Boiling Point | 169 °C(lit.) |
| Melting Point | 38-40 °C(lit.) |
| Molecular Formula | C38H46N4O6S |
| Molecular Weight | 686.860 |
| Flash Point | 148 °F |
| Exact Mass | 686.313782 |
| PSA | 155.70000 |
| LogP | 6.63300 |
| Index of Refraction | 1.717 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Mutation in the Plasmodium falciparum CRT protein determines the stereospecific activity of antimalarial cinchona alkaloids.
Antimicrob. Agents Chemother. 56(10) , 5356-64, (2012) The Cinchona alkaloids are quinoline aminoalcohols that occur as diastereomer pairs, typified by (-)-quinine and (+)-quinidine. The potency of (+)-isomers is greater than the (-)-isomers in vitro and ... |
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A theoretical investigation on the Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetraisopropyl titanate.
Chemistry 19(5) , 1637-46, (2013) The mechanism and the origin of selectivity of the asymmetric Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetrai... |
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Organocatalytic asymmetric conjugate addition of 3-monosubstituted oxindoles to (E)-1,4-diaryl-2-buten-1,4-diones: a strategy for the indirect enantioselective furanylation and pyrrolylation of 3-alkyloxindoles.
Chemistry 18(21) , 6679-87, (2012) An asymmetric conjugate addition of 3-monosubstituted oxindoles to a range of (E)-1,4-diaryl-2-buten-1,4-diones, catalyzed by commercially available cinchonine, is described. This organocatalytic asym... |
| Cinchonan-9-ol, (9S)-, sulfate (2:1) (salt) |
| (9S)-Cinchonan-9-ol sulfate (2:1) |
| EINECS 227-708-4 |
| MFCD00035639 |
| cinchonine sulfate |